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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1503146Generated: October 30, 2026

Sodium Cyanide → 3-(3-fluorophenyl)propanenitrile

https://huagongshe.com/reaction/1503146

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CyanideHCID 8929—
Reactant1-(2-Bromoethyl)-3-fluorobenzeneHCID 573129—
SolventDimethylformamideHCID 6228—
Product3-(3-fluorophenyl)propanenitrileHCID 1026124087%

Reaction Conditions

Temperature60 °C

Reaction Steps

3-Fluorophenethyl bromide (23, 1.00 g, 12.3 mmol) was diluted in dry DMF (25 mL). Sodium cyanide (1.06 g, 61.6 mmol) was added in one portion, and the mixture was heated to 60° C. under argon for 16 h. The mixture was cooled and concentrated, and the residue was partitioned between EtOAc and H2O (50 mL each). The layers were separated, and the aqueous phase was extracted with EtOAc (2×20 mL). The organic layers were washed with H2O and sat. aq. NaCl (50 mL each), dried over anhydrous sodium sulfate, and concentrated. The resulting oil was purified by flash column chromatography (SiO2), eluting with a gradient of 5% EtOAc in hexanes to 30% EtOAc in hexanes to yield the desired product as a colorless oil (0.638 g, 87%). 1H-NMR (500 MHz; CDCl3): δ 7.31 (td, J=7.9, 6.0 Hz, 1 H), 7.03-6.93 (m, 3 H), 2.96 (t, J=7.4 Hz, 2 H), 2.63 (t, J=7.4 Hz, 2 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09212144B2
Source datasetuspto-grants-2015_12
ORD IDord-e888f39008f34601ba259c862562d6eb
Source noteuspto-grants-2015_12